Lactotransferrin-Cre reporter mice trace neutrophils, monocytes/macrophages and distinct subtypes of dendritic cells
Boris Kovacic,
Andrea Hoelbl-Kovacic,
Katrin M. Fischhuber,
Nicole R. Leitner,
Dagmar Gotthardt,
Emilio Casanova,
Veronika Sexl,
Mathias Müller
Affiliations
Boris Kovacic
Institute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria;Research Institute of Molecular Pathology (I.M.P.), Vienna, Austria
Andrea Hoelbl-Kovacic
Institute of Pharmacology and Toxicology, University of Veterinary Medicine, Vienna, Austria
Katrin M. Fischhuber
Institute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria
Nicole R. Leitner
Institute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria
Dagmar Gotthardt
Institute of Pharmacology and Toxicology, University of Veterinary Medicine, Vienna, Austria
Emilio Casanova
Ludwig Boltzmann Institute for Cancer Research (LBI-CR), Vienna, Austria;Institute of Pharmacology, Center of Physiology and Pharmacology, Comprehensive Cancer Center, Medical University of Vienna, Austria
Veronika Sexl
Institute of Pharmacology and Toxicology, University of Veterinary Medicine, Vienna, Austria
Mathias Müller
Institute of Animal Breeding and Genetics, University of Veterinary Medicine Vienna, Vienna, Austria
Considerable effort has been expended to identify genes that account for myeloid lineage commitment and development. However, currently available non-invasive mouse models utilize myeloid-specific reporters that are significantly expressed in hematopoietic stem cells as well as lymphoid compartments. Here, we describe a myeloid-specific marker that is not shared by any other lineage. We show that lactotransferrin mRNA is expressed by Gr-1+/CD11b+ cells in the bone marrow, as opposed to hematopoietic stem cells or any peripheral cell population. To follow the progeny of lactotransferrin-expressing bone marrow cells, we generated a mouse model in which a reporter gene is irreversibly activated from the lactotransferrin-promoter. We found that lactotransferrin-reporter labels a majority of neutrophils, monocytes, macrophages and distinct subtypes of dendritic cells, while excluding T, B, natural killer cells, interferon-producing killer dendritic cells, plasmacytoid dendritic cells, erythrocytes and eosinophils. Lactotransferrin-reporter− bone marrow cells retain lymphoid, erythroid and long-term repopulating potential, while lactotransferrin-reporter+ bone marrow cells confer only myeloid, but not lymphoid potential. We conclude that lactotransferrin represents a late stage differentiation marker of neutrophils, macrophages and distinct subtypes of dendritic cells.